# Adkins, K. v. Johnson & Johnson

> Superior Court of Pennsylvania · April 15, 2020 · 231 A.3d 960

URL: https://www.frixlaw.com/law-library/cases/10782101

## Case

- **Court:** Superior Court of Pennsylvania
- **Decided:** April 15, 2020
- **Citations:** 231 A.3d 960; 2020 Pa. Super. 95
- **Precedential status:** Published
- **Opinion:** Opinion
- **Judges:** Olson
- **Cited by:** 1 later opinions in the Frix Law Library

## Citator (automated)

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## Opinion text

J-A17032-19

2020 PA Super 95

KIMBERLY L. ADKINS : IN THE SUPERIOR COURT OF
: PENNSYLVANIA
:
v. :
:
:
JOHNSON & JOHNSON, ETHICON, :
INC. INDIVIDUALLY AND D/B/A :
ETHICON, GYNECARE, SECANT : No. 2700 EDA 2017
MEDICAL, INC. SECANT MEDICAL, :
LLC, PRODESCO, INC. AND SECANT :
MEDICAL :
:
:
APPEAL OF: ETHICON, INC. AND :
JOHNSON & JOHNSON :

Appeal from the Order Entered July 19, 2017
In the Court of Common Pleas of Philadelphia County Civil Division at
No(s): July Term, 2013 No. 919

BEFORE: PANELLA, P.J., OLSON, J., and FORD ELLIOTT, P.J.E.

CONCURRING AND DISSENTING OPINION BY OLSON, J.: Filed: April 15, 2020

I agree with the learned Majority that Kimberly Adkins (“Adkins”) did

not waive her challenge to the weight of the evidence when she did not object

to the trial court’s jury instructions, verdict sheets, or the verdict itself. I am,

however, unable to agree with my learned colleagues that this panel should

affirm, in its entirety, the trial court’s order directing a new trial on the grounds

that the jury’s verdict was against the weight of the evidence. I agree with

my colleagues that a “no causation” finding as to Adkins’ claim for surgical

removal of the TCT SECUR pelvic mesh device (the “Device”) was against the

evidence since there was no explanation other than the presence of the

defective Device for why Adkins underwent surgical removal of the mesh
J-A17032-19

product. However, I would hold that, because Ethicon, Inc. and Johnson &

Johnson (collectively “Ethicon”) presented evidence at trial showing that

factors wholly unrelated to the Device may have caused Adkins’ pelvic

conditions, the jury’s “no causation” finding as to her claims for vaginal

bleeding, pelvic pain, vaginal pain, palpable mesh, dyspareunia, and mesh

exposure was not against the weight of the evidence. Accordingly, for the

reasons set forth below, I concur in part and dissent in part.

In large part, the Majority affirms the trial court’s determination that the

jury’s verdict was against the weight of the evidence because it finds that

“Ethicon’s causation expert agreed on cross-examination that the Device

caused certain of Adkins’ injuries.” Majority Opinion at 9. To reach this

conclusion, the Majority cites testimony offered by Ethicon’s causation expert

in which he agrees that from 2011 to 2012, “mesh-related” problems

experienced by Adkins included several conditions, including vaginal bleeding,

pelvic pain, vaginal pain, pain during intercourse, scratching of her sexual

partner, mesh exposure, and surgical removal. See id. at 9-10. On the

strength of this testimony, the Majority concludes that “[t]he record clearly

demonstrates that it was undisputed that from 2011 to 2012, the erosion of

the mesh as found to be a defect by the jury caused Adkins to suffer [from

the foregoing injuries and conditions].” Id. at 10. In the Majority’s view, the

jury’s “no causation” finding was against the weight of the evidence because

there was “no[] conflict in the testimony with respect to the injuries the Device

caused in 2011 to 2012[.]” Id.

-2-
J-A17032-19

Unlike the Majority, I do not believe that the evidence, particularly the

single exchange lifted from the cross-examination testimony of Ethicon’s

causation expert, produced such clear cut support of a causation verdict

favorable to Adkins and justified the trial court casting aside the jury’s finding

on causation. As the Majority acknowledges, the substantive principles of

Ohio product liability law that govern this dispute require a plaintiff to show

both a defect in the product manufactured and sold by the defendant and

that the defect directly and proximately caused the plaintiff’s injuries

and losses. See Majority Opinion at 8-9 (citing cases). The jury here found

that the Device was defectively designed and that the warnings given by

Ethicon were inadequate; however, the jury rejected a finding that a defect in

the Device proximately caused any injury sustained by Adkins.

As a preliminary matter, the plain language of the sole exchange of

expert testimony cited by the Majority did not contradict the jury’s finding that

causation was unproven. In the cited passage, Ethicon’s expert agreed that,

from 2011 through 2012, Adkins experienced various conditions that were

“mesh-related.” See id. at 9, citing N.T. Trial, 6/7/17, at 66. Notwithstanding

this response, the fact that an injury or condition may be “mesh-related” does

not mean that a defect in the mesh was the proximate cause of an injury. A

condition may be “mesh-related” because it resulted from the surgical mesh

implantation procedure or because the condition and the implant are both

located in the same part of Adkins’ anatomy. In short, given the ambiguity of

the terms employed in the question, it was for the jury to decide whether the

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J-A17032-19

words “mesh-related” meant “produced or caused by a defect in the mesh” or

referred to some other non-causal connection between the mesh and Adkins’

conditions.

Inferential arguments in support of setting aside the jury’s

determination and awarding a new trial on grounds that the verdict was

against the weight of the evidence are even less persuasive in view of the

substantial evidence and testimony which tended to establish that several

factors unrelated to the Device (and, more specifically, unrelated to any

alleged defects in the Device), including implantation procedures, Adkins’

smoking history, tissue atrophy, non-adherence to post-surgical instructions,

and the lack of feasible alternative designs that would have avoided any

alleged risks, led to the injuries sustained by Adkins.1 See Ethicon’s Brief at

33-34 and 40. Ethicon thus asserts that the verdict was not contrary to the

____________________________________________

1 In fact, the same defense expert cited by the Majority in support of its
conclusion also testified that Adkins’ vaginal tissue erosion in 2012 was a
known risk of her surgical procedure that could be explained by poor wound
healing characteristics, smoking, tissue atrophy, and age. See N.T. Trial,
6/7/17, at 78-80 (“So basically, there’s medical conditions [such as smoking
and poor wound healing], there’s local factors like atrophy, and there’s sort of
like following the rules to let things heal well. And as a basic outline, those
are the things that would increase the risk for erosion.”). In view of this
extensive testimony, it would not be accurate, in my assessment, to
characterize the cited excerpt of the expert’s opinion as a concession that a
defect in the Device acted as the proximate cause of all of Adkins’ injuries and
losses. Instead, the record, viewed as a whole, reflects that several factors
were presented to the jury as potential causes of Adkins’ alleged conditions
and damages. Within the context of the hotly contested dispute before us,
the fact that the jury credited one or more causation factors that were not
favorable to Adkins does not support the conclusion that the verdict was
shocking or that a new trial is warranted.

-4-
J-A17032-19

evidence because the jury heard evidence that Adkins’ conditions and

damages were not caused by defects in the Device. Against the factual record

developed at trial, and bearing in mind the relevant principles of tort law, I

am reluctant to conclude, as the Majority seems to do, that the agreement by

Ethicon’s causation expert that Adkins sustained “mesh-related” problems

between 2011 and 2012 equates to a concession that defects in the Device

were a direct and proximate cause of Adkins’ injuries and losses. Compare

Majority Opinion at 10.

Less obvious is the unstated line of reasoning gleaned from the

Majority’s rationale. After reciting an exchange in which Ethicon’s expert

agreed that Adkins experienced “mesh-related” problems from 2011 through

2012, the Majority concludes that “the erosion of the mesh as found to be

defective by the jury caused Adkins to suffer the following injuries: vaginal

bleeding, pelvic pain, vaginal pain, palpable mesh, pain with sex, and mesh

exposure in her vagina. There is no dispute that because the Device caused

these injuries, Adkins had to undergo surgical removal of the device.” Majority

Opinion at 10 (emphasis added). The Majority’s logic is clear, if not expressly

stated: if a product later found to be defective has been linked to injuries, it

follows, a fortiori, that a defect in the product must have been the proximate

cause of all of the injuries with which it is associated.

I cannot agree with this rationale given the record in this case. Merely

linking a defective product to an injury, loss, or condition is simply not the

same as demonstrating its causal connection to alleged damages. Here, the

-5-
J-A17032-19

jury heard substantial evidence explaining why a defect in the Device did not

cause most of Adkins’ conditions. In the face of such evidence, I am not

convinced that the jury’s “no causation” finding for the majority of Adkins’

conditions ran contrary to the weight of the evidence.2

I realize that we must give the gravest consideration to the findings and

reasons advanced by a trial judge when reviewing a determination that a

verdict was against the weight of the evidence. I also recognize that this is

one of the least assailable rulings that can be issued by a trial court. See

Brown v. Trinidad, 111 A.3d 755, 770 (Pa. Super. 2015). However, under

the facts and circumstances of this case, I cannot agree that the trial court

properly exercised its discretion when it granted a new trial as to all of Adkins’

alleged losses and damages. Thus, I must respectfully concur in part and

dissent in part.

____________________________________________

2 As there was no evidence of alternative reasons for removing the defective

Device, I would agree that the jury’s “no causation” finding as to surgical
removal of the Device (as a condition or loss separate from the other vaginal
conditions) was against the weight of the evidence. Hence, I would award a
new trial limited to this claim.

-6-

---

Source: Frix Law Library, https://www.frixlaw.com/law-library/cases/10782101. Public record. Not legal advice.
